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Molecular Mechanisms Mediating Gibberellin-Induced Parthenocarpic Fruit Development in Grapevines (Vitis spp.)

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Authors

허윤영

Advisor
이희재
Major
농업생명과학대학 식물생산과학부
Issue Date
2014-08
Publisher
서울대학교 대학원
Keywords
AuxinAuxin response factorGibberellinGibberellin methyltransferaseGibberellin oxidaseGrapevine inflorescenceParthenocarpySeedlessness
Description
학위논문 (박사)-- 서울대학교 대학원 : 식물생산과학부, 2014. 8. 이희재.
Abstract
The concept that gibberellin (GA) application on seeded grapevines induces parthenocarpy has been known for decades in viticulture, but the molecular mechanism underlying this induction is poorly understood. GA was applied to inflorescence clusters of seeded diploid grapevine cultivar Tamnara (Vitis spp.) at 14 days before full bloom (DBF). Morphological and molecular effects of GA application were examined on the induction of parthenocarpic fruit development. With GA application, ovaries were enlarged and pollen tube growth was completely inhibited. Vitis GA oxidases, the key determinants for GA level, were characterized through phylogenetic analysis with Arabidopsis GA oxidase. Five VvGA 20-oxidase (VvGA20ox), three VvGA 3-oxidase (VvGA3ox), and nine VvGA 2-oxidase (VvGA2ox) family proteins, and one VvGA methyltransferase (VvGAMT) and one Vitis cytochrome P450 (VvCYP) 714A proteins were identified, and their expression patterns were analyzed during inflorescence development from 14 DBF to 5 days after full bloom (DAF). VvGA2ox1, VvGA20ox3, and VvGA3ox2 transcripts were most abundantly expressed in each gene family at 7, 5, and 2 DBF, respectively. Following GA application at 14 DBF inducing seedlessness, GA catabolic genes such as VvGAMT2, VvGA2ox3, and VvGA2ox4 were up-regulated at 12 DBF, full bloom, and 5 DAF, respectively. Conversely, GA biosynthetic genes, VvGA20oxs and VvGA3oxs, were down-regulated at near full bloom, and the timing of their peak expression was changed. These results suggest that GA application at pre-bloom changes the GA biosynthesis into GA catabolic pathway at near full bloom by altering the transcript level and timing of GA oxidase genes expression during grapevine inflorescence development. In addition, the transcriptional levels of the putative negative regulators of fruit set initiation, including Vitis auxin/indole-3-acetic acid transcription factor 9 (VvIAA9), Vitis auxin response factor 7 (VvARF7), and VvARF8 were also monitored during inflorescence development. Without GA application, VvIAA9, VvARF7, and VvARF8 were expressed at a relatively high level before full bloom, but decreased thereafter following pollination. However, after GA application at 14 DBF, the expression levels of VvIAA9 and VvARF7 declined at 5 DBF prior to pollination. The effects of GA application on auxin levels or auxin signaling were also analyzed by monitoring the expression patterns of auxin-biosynthetic and -responsive genes with or without GA application. Transcript levels of the auxin biosynthetic genes of Vitis anthranilate synthase β subunit (VvASB1-like), Vitis YUCCA2 (VvYUC2), and VvYUC6 were not significantly changed by GA application. However, the expressions of Vitis Gretchen Hagen3.2 (VvGH3.2) and VvGH3.3, auxin-responsive genes, were up-regulated from 2 DBF to full bloom with GA application. Furthermore, the Vitis GA signaling gene, VvDELLA was up-regulated by GA application during 12 to 7 DBF, prior to down-regulation of VvIAA9 and VvARF7. These results suggest that VvIAA9 and VvARF7 are negative regulators of fruit set initiation in grapevines, and GA signaling is integrated with auxin signaling via VvDELLA during parthenocarpic fruit development in grapevines.
Language
English
URI
https://hdl.handle.net/10371/120992
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